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猪细小病毒YK株NS1基因的克隆与序列分析
引用本文:白红光,卫广森,徐宏军,李尚波,王文成.猪细小病毒YK株NS1基因的克隆与序列分析[J].中国兽医科学,2005,35(8):615-619.
作者姓名:白红光  卫广森  徐宏军  李尚波  王文成
作者单位:1. 沈阳农业大学,畜牧兽医学院,辽宁,沈阳,110161
2. 中国农业科学院,兰州兽医研究所,甘肃,兰州,730046
3. 辽宁益康生物制品厂,辽宁,辽阳,111000
摘    要:提取猪细小病毒(PPV)YK株基因组DNA,利用PCR技术扩增得到了NS1基因全序列,将其克隆到pMD18-T质粒载体并进行了序列测定和分析。结果表明,NS1基因全长1989bp,编码662个氨基酸。氨基酸序列中含有在PPV复制过程中起重要作用的保守基序GKRN,并有3个潜在的糖基化位点NISN、NFSN和NLTR。PPVYK株的NS1基因与其他PPV毒株NADL-2(4973)株、NADL-2(5075)株、NADL-2(5034)株和Kresse株相比,核苷酸同源性分别为98.3%、99.9%、99.9%和99.7%,氨基酸同源性分别为99.7%、99.7%、99.7%和97.7%。结果说明,NS1基因具有高度保守性。

关 键 词:猪细小病毒  NS1基因  克隆
文章编号:1000-6419(2005)08-0615-05
修稿时间:2005年4月25日

Cloning and sequence analysis of NS1 gene of porcine parvovirus YK strain
BAI Hong-guang,WEI Guang-sen,XU Hong-jun,LI Shang-bo,WANG Wen-cheng.Cloning and sequence analysis of NS1 gene of porcine parvovirus YK strain[J].Veterinary Science in China,2005,35(8):615-619.
Authors:BAI Hong-guang  WEI Guang-sen  XU Hong-jun  LI Shang-bo  WANG Wen-cheng
Institution:BAI Hong-guang~
Abstract:The genomic DNA of PPV-YK strain was extracted. The whole NS1 gene was obtained by PCR,and cloned into pMD18-T for sequence. It was found that NS1 gene of PPV-YK strain is composed of 1989 nucleotides, and encodes 662 amino acids. NS1 protein of PPV-YK strain contains the conserved sequence GKRN that is important in replication of PPV. There are three potential N-glycosylation sites NISN,NFSN and NLTR in NS1 protein of PPV-YK strain. NS1 gene of PPV-YK strain shared 98.3%,99.9%,99.9% and 99.7% identity of nucleotide sequence and 97.7%,99.7%, (99.7%) and 99.7% identity of amino acid sequence with that of NADL2(4973) strain,NADL2(5075) strain,NADL2(5034) strain and Kresse strain,respectively. The results showed that NS1 gene is highly conservative.
Keywords:porcine parvovirus  NS1 gene  cloning
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